Due to the barriers imposed by the restriction-modification (RM) system, Nisin-producing industrial strains of often encounter low transformation efficiency, which seriously hinders the widespread application of genetic engineering in non-model . Herein, we present a novel pre-modification strategy (PMS) coupled with optimized plasmid delivery systems designed to systematically evade RM barriers and substantially improve Nisin biosynthesis in . Through the use of engineered strains with methylation profiles specifically optimized for C20, we have effectively evaded RM barriers, thereby facilitating the efficient introduction of large Nisin biosynthetic gene clusters into . The PMS tools, which significantly improve the transformation efficiency (~10 transformants per microgram of DNA), have been further improved in combination with a Rolling Circle Amplification, resulting in a higher enhancement in transformation efficiency (~10 transformants per microgram of DNA). Using this strategy, large Nisin biosynthetic gene clusters and the expression regulation of all genes within the cluster were introduced and analyzed in , leading to a highest Nisin titer of 11,052.9 IU/mL through a fed-batch fermentation in a 5 L bioreactor. This is the first systematic report on the expression regulation and application of a complete Nisin biosynthesis gene cluster in . Taken together, our studies provide a versatile and efficient strategy for systematic evasion and enhancement of RM barriers and Nisin biosynthesis, thereby paving the way for genetic modification and metabolic engineering in .
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http://dx.doi.org/10.3390/ijms26052200 | DOI Listing |
Foods
February 2025
College of Life Science, Dalian Minzu University, Dalian 116600, China.
Pumpkin is rich in nutritional value, and it can be eaten as a vegetable or as a staple food, making it popular among modern consumers. However, after fresh cutting, pumpkins are susceptible to moisture loss, softening, microbial contamination, and browning, all of which significantly compromise their quality during storage. Therefore, it is essential to develop effective preservation techniques for maintaining the quality of fresh-cut pumpkins.
View Article and Find Full Text PDFInt J Mol Sci
February 2025
School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China.
Due to the barriers imposed by the restriction-modification (RM) system, Nisin-producing industrial strains of often encounter low transformation efficiency, which seriously hinders the widespread application of genetic engineering in non-model . Herein, we present a novel pre-modification strategy (PMS) coupled with optimized plasmid delivery systems designed to systematically evade RM barriers and substantially improve Nisin biosynthesis in . Through the use of engineered strains with methylation profiles specifically optimized for C20, we have effectively evaded RM barriers, thereby facilitating the efficient introduction of large Nisin biosynthetic gene clusters into .
View Article and Find Full Text PDFMicroorganisms
February 2025
Nissin York Co., Ltd., 3-6-11 Higashi-Nihonbashi Chuo-ku, Tokyo 103-0004, Japan.
T-21 is a lactic acid bacterium isolated from wild cranberries in Japan that demonstrates significant immunomodulatory properties and has been incorporated into commercial health products. However, probiogenomic analyses specific to T-21 have remained largely unexplored. This study performed a thorough genomic characterisation of T-21 and evaluated its safety in initial clinical trials.
View Article and Find Full Text PDFWorld J Microbiol Biotechnol
February 2025
Food Technology Division, Bhabha Atomic Research Centre, Trombay, Mumbai, India.
DNA-binding proteins like Dps are crucial for bacterial stress physiology. This study investigated the unexpected role of Dps protein in maintaining outer membrane integrity of Salmonella Typhimurium. We observed that a Δdps mutant displayed increased sensitivity to glycopeptide antibiotics (vancomycin, nisin), which are ineffective against Gram-negative bacteria due to their thick outer membrane (OM).
View Article and Find Full Text PDFMicrobiology (Reading)
February 2025
Quadram Institute Bioscience, Norwich Research Park, Norwich, UK.
Nisin O is an antimicrobial peptide encoded by the human gut bacterium A2-162 which has antimicrobial activity against clinically relevant organisms. The nisin O biosynthetic gene cluster (BGC) varies from other nisin BGCs as it lacks a leader-peptide cleaving protease and contains two bacterial two-component response regulator-histidine kinase (RK) systems. The dissemination of the nisin O cluster, the final proteolytic biosynthesis step and the regulation of nisin O are currently unknown and are the foci of this study.
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